People with Down syndrome (DS) are at high risk for developing Alzheimer disease (AD). Neuropathology consistent with AD is present by 40 years of age and dementia may develop up to a decade later. In this review, we describe metabolic and vascular neuroimaging studies in DS that suggest these functional changes are a key feature of aging, linked to cognitive decline and AD in this vulnerable cohort. FDG-PET imaging in DS suggests systematic reductions in glucose metabolism in posterior cingulate and parietotemporal cortex. Magentic resonance spectroscopy studies show consistent decreases in neuronal health and increased myoinositol, suggesting inflammation. There are few vascular imaging studies in DS suggesting a gap in our knowledge. Fut...
Abstract People with Down syndrome (DS) are at high risk for developing Alzheimer disease (AD) with ...
Individuals with Down syndrome (DS) are more likely to experience earlier onset of multiple facets o...
AbstractTo determine if proton magnetic resonance spectroscopy (1H-MRS) detect differences in dement...
People with Down syndrome (DS) are at high risk for developing Alzheimer disease (AD). Neuropatholog...
People with Down syndrome (DS) are at high risk for developing Alzheimer disease (AD). Neuropatholog...
ObjectiveAdults with Down syndrome (DS) develop Alzheimer disease (AD) pathology by their 5th decade...
People with Down syndrome (DS) develop Alzheimer's disease (AD) at higher rates and a younger age of...
BackgroundPeople with Down syndrome (DS) develop Alzheimer's disease (AD) at an earlier age of onset...
Epidemiological evidence suggests that by the age of 40 years, all individuals with Down syndrome (D...
OBJECTIVE: Down's syndrome is characterized by the genetically programmed accumulation of substantia...
IntroductionDisruption of metabolic function is a recognized feature of late onset Alzheimer's disea...
Down syndrome (DS) is a common cause of intellectual disability and is also associated with early ag...
Epidemiological evidence suggests that by the age of 40 years, all individuals with Down syndrome (D...
To gain further knowledge on the preclinical phase of Alzheimer's disease (AD), we sought to charact...
People with Down syndrome (DS) are at high risk for developing Alzheimer disease (AD) with age. Typi...
Abstract People with Down syndrome (DS) are at high risk for developing Alzheimer disease (AD) with ...
Individuals with Down syndrome (DS) are more likely to experience earlier onset of multiple facets o...
AbstractTo determine if proton magnetic resonance spectroscopy (1H-MRS) detect differences in dement...
People with Down syndrome (DS) are at high risk for developing Alzheimer disease (AD). Neuropatholog...
People with Down syndrome (DS) are at high risk for developing Alzheimer disease (AD). Neuropatholog...
ObjectiveAdults with Down syndrome (DS) develop Alzheimer disease (AD) pathology by their 5th decade...
People with Down syndrome (DS) develop Alzheimer's disease (AD) at higher rates and a younger age of...
BackgroundPeople with Down syndrome (DS) develop Alzheimer's disease (AD) at an earlier age of onset...
Epidemiological evidence suggests that by the age of 40 years, all individuals with Down syndrome (D...
OBJECTIVE: Down's syndrome is characterized by the genetically programmed accumulation of substantia...
IntroductionDisruption of metabolic function is a recognized feature of late onset Alzheimer's disea...
Down syndrome (DS) is a common cause of intellectual disability and is also associated with early ag...
Epidemiological evidence suggests that by the age of 40 years, all individuals with Down syndrome (D...
To gain further knowledge on the preclinical phase of Alzheimer's disease (AD), we sought to charact...
People with Down syndrome (DS) are at high risk for developing Alzheimer disease (AD) with age. Typi...
Abstract People with Down syndrome (DS) are at high risk for developing Alzheimer disease (AD) with ...
Individuals with Down syndrome (DS) are more likely to experience earlier onset of multiple facets o...
AbstractTo determine if proton magnetic resonance spectroscopy (1H-MRS) detect differences in dement...